Analysis of the binding mode of laulimalide to microtubules: Establishing a laulimalide-tubulin pharmacophore

作者：Churchill Cassandra D M; Klobukowski Mariusz; Tuszynski Jack A^*

来源：Journal of Biomolecular Structure & Dynamics, 2016, 34(7): 1455-1469.

DOI：10.1080/07391102.2015.1078115

• laulimalide
• isolaulimalide
• rational drug design
• cytotoxicity
• microtubule
• tubulin heterodimer

Laulimalide (LA) is a microtubule-stabilizing agent, currently in preclinical studies. However, studying the binding of this species and successfully synthesizing potent analogues have been challenging. The LA binding site is located between tubulin protofilaments, and therefore LA is in contact with two adjacent -tubulin units. Here, an improved model of the binding mode of LA in microtubules is presented, using the newly available crystal structure pose and an extended tubulin heterodimer complex, as well as molecular dynamics simulations. With this model, a series of LA analogues developed by Mooberry and coworkers are also analyzed in order to establish important pharmacophores in LA binding and cytotoxicity. In the side chain, interactions are important contributors to LA binding, as are water-mediated hydrogen bonds. An intramolecular hydrogen bond is correlated with high cytotoxicity, and is dependent on macrocycle conformation. Therefore, while the epoxide and olefin groups in the macrocycle do not engage in specific interactions with the protein, they are essential contributions to an active macrocycle conformation, and therefore potency. Calculations reveal that a balance in binding affinity is important for LA activity, where the more potent compounds have larger interactions with the adjacent tubulin unit than the less-active analogs. Several modifications are suggested for the rational design of LA analogues that should not disrupt the active macrocycle conformation.

• 出版日期2016
• 单位Saskatchewan